Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Kearns-Sayre Syndrome	[NCBI]

Gene	Link	Information Gain
TRNL1	[NCBI]	0.000576076
CASQ1	[NCBI]	1.49174e-05
ATXN7	[NCBI]	1.30304e-05
LBR	[NCBI]	1.26056e-05
CS	[NCBI]	1.05555e-05
KCNQ1	[NCBI]	9.01119e-06
PTGS2	[NCBI]	4.58671e-06

OMIM	Link	Information gain
KSS	[NCBI]	0.010809
pearson marrow-pancreas syndrome	[NCBI]	0.000289594
MTTL1	[NCBI]	0.0002016
mitochondrial complex ii deficiency	[NCBI]	6.32629e-05
MTTK	[NCBI]	6.11901e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive	[NCBI]	5.27622e-05
MELAS	[NCBI]	4.08382e-05
LS	[NCBI]	2.18008e-05
RP	[NCBI]	4.29091e-07